LivingGLP1
Study S002029

A Randomized Clinical Trial to Study Glucose Dependent Insulin Secretion Methodologies in Healthy Lean Male Subjects

Registration

Registration
NCT00782418
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
27
Start
2008-09
Primary completion
2009-02
Lead sponsor
Merck Sharp & Dohme LLC
Conditions
The Methodology Assessment of Glucose Dependent Insulin Secretion
Interventions
DRUG:Comparator: exenatide; DRUG:Comparator: Placebo
Results posted
TRUE
Secondary identifiers
OTHER:2008_568

Registered primary outcomes

  • Change From Baseline in Insulin Secretion Rate (ISR) Normalized to Ambient Plasma Glucose [Steady-state of HGC: 90 - 120 minutes post dose; highest glucose infusion rate of GGI: 120 - 160 minutes post dose]
  • Change From Baseline in C-peptide Concentration [Pre and Post glucose infusion]
  • Change From Baseline in Insulin Concentration [Pre and Post glucose infusion]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0028793Linearity of β-cell response across the metabolic spectrum and to pharmacology: insights from a graded glucose infusion-based investigation series.
Shankar SS, American journal of physiology. Endocrinology and metabolism
2016Other trialPMID 27072496DOIcites ClinicalTrials.gov:NCT00782418; registry reference RESULT:27072496